Skip to Content
MilliporeSigma
All Photos(1)

Documents

193941

Sigma-Aldrich

4-Chlorophenoxyacetyl chloride

98%

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
ClC6H4OCH2COCl
CAS Number:
Molecular Weight:
205.04
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

98%

refractive index

n20/D 1.5486 (lit.)

bp

142 °C/17 mmHg (lit.)

mp

18.8 °C (lit.)

density

1.314 g/mL at 25 °C (lit.)

SMILES string

ClC(=O)COc1ccc(Cl)cc1

InChI

1S/C8H6Cl2O2/c9-6-1-3-7(4-2-6)12-5-8(10)11/h1-4H,5H2

InChI key

VRBVHQUSAOKVDH-UHFFFAOYSA-N

Application

4-Chlorophenoxyacetyl chloride was used in the preparation of:
  • substituted acetophenone derivatives
  • 2-(4-chlorophenoxyacetylamino)-3-ethoxycarbonyl[2,3-b]quinuclidine
  • 2-(4-chlorophenoxy)-N′-[2-(4-chlorophenoxy)acetyl]acetohydrazide monohydrate

pictograms

Corrosion

signalword

Danger

hcodes

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Ting Chen et al.
Acta crystallographica. Section E, Structure reports online, 66(Pt 11), o2829-o2829 (2010-01-01)
In the title compound, C(16)H(14)Cl(2)N(2)O(4)·H(2)O, the hydrazine and water mol-ecules are both located on twofold axes. The C-N-N-C torsion angle is -72.66 (1)° and the dihedral angle between the two benzene rings is 67.33 (1)°. In the crystal, mol-ecules are linked into
Synthesis and properties of 2-amino-3-ethycarbonylthieno [2, 3-b] quinuclidines.
Kaminka ME, et al.
Pharmaceutical Chemistry Journal, 21(8), 568-570 (1987)
Jonathan Rosen et al.
Organic letters, 9(4), 667-669 (2007-01-27)
A direct and efficient method was developed for the preparation of a variety of substituted acetophenone derivatives from readily available arene precursors and acid chlorides. This method has significant generality and affords access to substitution patterns on aryl rings not

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service